Area of research
Immunology · Molecular Biology
Research interest
Research interests include Immunotherapy and Immune Responses, RNA Interference and Gene Delivery, Nanoparticle-Based Drug Delivery, and CAR-T cell therapy research.
Viral vector-based gene therapies in the clinic: An update.
Polyplex of peptide-mannan and RNA for intranasal delivery of TGF-β siRNA in treatment of pulmonary fibrosis
Integrating antigen capturing nanoparticles and type 1 conventional dendritic cell therapy for in situ cancer immunization
Stem cell therapies in the clinic
Integrating antigen capturing nanoparticles and type 1 conventional dendritic cell therapy for in situ cancer immunization.
Nanoparticle-boosted myeloid-derived suppressor cell therapy for immune reprogramming in multiple sclerosis
Cell therapies against brain tumors: Clinical development and emerging prospects
Stem cell therapies in the clinic.
Adoptive T‐cell therapies in the clinic
Adoptive T‐cell therapies in the clinic
Nanoparticle-boosted myeloid-derived suppressor cell therapy for immune reprogramming in multiple sclerosis.
PEGylated therapeutics in the clinic.
Hydrogels in the clinic: An update
Hydrogels in the clinic: An update.
In situ cellular hitchhiking of nanoparticles for drug delivery
Vaccine adjuvants for infectious disease in the clinic
Cancer vaccines in the clinic.
Vaccine adjuvants for infectious disease in the clinic.
Antibody drug conjugates in the clinic
Phalloidin-PAINT: Enhanced quantitative nanoscale imaging of F-actin
Antibody drug conjugates in the clinic.
Genetically engineered cell-derived nanovesicles for cancer immunotherapy
Genetically engineered cell-derived nanovesicles for cancer immunotherapy.
Quantitative Superresolution Imaging of F-Actin in the Cell Body and Cytoskeletal Protrusions Using Phalloidin-Based Single-Molecule Labeling and Localization Microscopy
<scp>PEGylated</scp> therapeutics in the clinic
Alzheimer's and Parkinson's disease therapies in the clinic.
Cancer vaccines in the clinic
Systemic Tumor Suppression via Macrophage‐Driven Automated Homing of Metal‐Phenolic‐Gated Nanosponges for Metastatic Melanoma